| Literature DB >> 26892026 |
Jane E Haley1, Anthony H Dickenson2.
Abstract
We used in vivo electrophysiology and a model of more persistent nociceptive inputs to monitor spinal cord neuronal activity in anaesthetised rats to reveal the pharmacology of enhanced pain signalling. The study showed that all responses were blocked by non-selective antagonism of glutamate receptors but a selective and preferential role of the N-methyl-d-aspartate (NMDA) receptor in the prolonged plastic responses was clearly seen. The work lead to many publications, initially preclinical but increasingly from patient studies, showing the importance of the NMDA receptor in central sensitisation within the spinal cord and how this could relate to persistent pain states. This article is part of a Special Issue entitled SI:50th Anniversary Issue.Entities:
Keywords: Central sensitisation; N-methyl-d-aspartate (NMDA) receptors; Pain; Spinal cord
Mesh:
Substances:
Year: 2016 PMID: 26892026 DOI: 10.1016/j.brainres.2016.02.001
Source DB: PubMed Journal: Brain Res ISSN: 0006-8993 Impact factor: 3.252